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FLEX-TECH BALLOON DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K926038
510(k) Type
Traditional
Applicant
CAPE TECH MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1993
Days to Decision
328 days
Submission Type
Statement

FLEX-TECH BALLOON DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K926038
510(k) Type
Traditional
Applicant
CAPE TECH MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1993
Days to Decision
328 days
Submission Type
Statement